Neonatal Flashcards

1
Q

Gastroschisis Description

A

defect in anterior abdo wall lateral to umbilicus

herniated intestine /w no covering/sac

no associated abnormalities

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2
Q

omphalocele

A

incomplete closure of ant abdo wall

herniated bowel, stomach, liver, spleen in peritoneal sac

often other abnormalities

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3
Q

NRP algorithim

A

dry, stimulate, clear secretions (30secs)

if apnea, gasping or HR < 100: PPV, SpO2 monitor, +/- ECG

HR < 100? Check chest movement, correct PPV. ETT or LMA if needed.

then if HR <60, ETT. Compressions. 100% O2. ECG monitor.

HR still <60, IV epi

HR persistently <60, consider hypovolemia or pneumothorax

if labored breathing or persistent cyanosis only: position + clear airway, supplemental O2 PRN. Consider CPAP.

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4
Q

Preductal SpO2 targets in newborn resusc

A
1min - 60-65%
2min - 65-70%
3 min - 70-75%
4 min - 75-80%
5 min - 80 - 85%
10 min - 85-95%
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5
Q

changes at birth in circulation

A

hypoxia –> breath

breathing/O2 –> lower pulm resistance, increased pulm blood flow

loss of placental circulation –> increased systemic vascular resistance, closing FO + DA

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6
Q

prematurity acute + chronic morbidity

A

acute:

  • CNS: asphyxia, IVH, seizures, periventricular leukomalacia
  • Resp: RDS, apnea of prematurity (monitoring until 5-8d without apnea)
  • CVS: PDA
  • GI: feeding intolerance, NEC
  • ID: sepsis
  • Derm: temp instability

chronic:

  • HEENT: ROP, hearing impairment
  • Resp: CLD
  • CNS: behavioural, LDs, CP, cognitive, seizures
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7
Q

management of late preterm infants (34+)

A

<35 need NICU, otherwise may not

observe - temp, jaundice, BG, car seat test

careful monitor feeding, weight gain until consistent

risk of readmission

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8
Q

kernicterus diagnosis

A

only dx on histology (see in basal ganglia)

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9
Q

acute bilirubin encephalopathy diagnosis

A

= clinical diagnosis

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10
Q

physiologic causes of jaundice

A

breast feeding jaundice (=not getting enough)

breast milk jaundice (getting enough but reacting to a component)

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11
Q

Pathologic causes of Jaundice

A

Unconjugated/indirect

  • hemolytic: ABO incompatible, fragmentation, spherocytosis/elliptocytosis, G6PD def, PKD, alpha thalassemia
  • others: cephalohematoma, bruising, craig najar syndrome, gilberts, sepsis, hypothyroidism

Conjugated/direct

  • biliary atresia
  • choledocal cysts
  • infections: sepsis, viral, TORCH, UTI
  • metabolic: galactosemia, A1AT def, hypothyroidism
  • long term TPN
  • idiopathic neonatal hepatitis
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12
Q

Jaundice work up

A

universal:

  • TSB before discharge / 72h
  • blood type & screen
  • baby blood type
  • G6PD if ethnic group (consider)

If severe/treating:

  • DAT (coombs)
  • CBC + diff
  • smear & retics
  • unconj + conj serum bili
  • G6PD - if asian or severe
  • consider septic w/u (eg if WBC off, etc)

Note: also do DAT if high-intermed risk and mom is group O

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13
Q

Jaundice likely pathologic if

A
  • jaundice at <24hr
  • bili rises rapidly or very high
  • persists beyond 2 weeks
  • conjugated hyperbilirubinemia (does not cause kernicterus or respond to phototherapy – but must workup!)
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14
Q

treatment for hyperbilirubinemia

A
  • phototherapy (blanket, light)

- if severe, IVIG, partial exchange transfusion

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15
Q

how to dx hyperbilirubinemia

A
  • use nomogram of total bili to decide if phototherapy
  • if no tx, then use 2nd nomogram to determine risk zone + follow-up needed
  • RFs = iso immune hemolytic dx, G6PD, asphyxia, resp distress, lethargy, temp instability, sepsis, acidosis

lines: 38+well, 35-38 + wll or term /w RFs, 35-38 with RFs

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16
Q

signs of kernicterus

A

hypertonia, arcing, retrocolis, fever, opthisthotonos, high pitched cry

17
Q

tx of kernicterus

A

exchange transfusion

18
Q

risk factors for neonatal sepsis

A
ROM > 18hr
intrapartum fever
maternal GBS
prev infant with GBS
chorioamnionitis
prematurity
perinatal asphyxia
19
Q

micro-organisms for neonatal sepsis

A
GBS
E coli
Strep Viridans
Strep pneumo
enterobacter
S aureus
H flu
HSV
enteroviruses
20
Q

presentation of neonatal sepsis

A
non-specific/subtle
poor feeding
lethargy
vomiting
resp distress/grunting/apnea
temp instability
low tone
tachycardia
fever or hypothermia
seizures
petechiae
21
Q

full septic workup

A
CBC
blood cultures
urinalysis + culture
LP - CSF anlalysis, culture, viral PCR
\+/- CXR, stool testing
22
Q

when to do a workup for sepsis

A

unwell - full w/u

well and multiple RF or chorio: do CBC after 4 hrs

one RF: observe for 24hr, +/- CBC

23
Q

empiric antibiotics for neonatal sepsis

A

ampicillin + gent or cefotaxime

add vanco if >30d, if ?meningitis, or if lines in

add acyclovir if ?HSV

24
Q

Ddx for neonatal resp distreass

A

most common:

  • transient tachypnea of newborn
  • respiratory distress syndrome
  • meconium aspiration syndrome

less common:

  • infection (pneumonia, sepsis)
  • persistent pulmonary HTN
  • pneumothorax, effusion, lung hemorrhage
25
investigation for neonatal resp distress
CBC, lytes, BG, blood gas, blood cultures LP if ?sepsis, meningitis CXR echo (esp if severe hypoxemia or ?PPHN) ECG pre and post ductal sats (PPHN)
26
Transient tachypnea of Newborn description, dx, treatment
"wet lungs" RF: CS, macrosomia, maternal DM CXR: parenchymal infiltrates, wet silhouette, intralobal fluid tx: give O2 PRN
27
Respiratory Distress Syndrome
not enough surfactant RF: male, maternal DM, preterm tachypnea, hypoxia, cyanosis CXR: homogenous infiltrates, air bronchograms, small volumes tx: resusc, O2, ventilate, give surfactant
28
mec aspiration syndrome
post-term, SGA patchy atelectatsis, consolidation resusc, O2, ventilate, surfactant if severe, abx until cultures back (b/c looks like pneumonia)
29
neonatal hypoglycemia cut off
<2.6
30
neonatal hypoglycemia causes
endocrine: persistent hyperinsulinemic hypoglycemia of infancy, diabetic mom, LGA, other rare things ``` perinatal stress sepsis RDS prematurity PPHN rare inborn errors of metabolism ```
31
work-up for persistent hypoglycemia / requiring lots of glucose
"critical labs" - PG - blood gas - insulin level - GH - cortisol - FFA - beta-hydroxybutarate - acyclcarnitinse - total and free carnitine - serum amino acids - ammonia - lactate - c-peptide - urine: ketones, glucose, organic acids, reducing substrates
32
management of neonatal hypoglycemia
LGA + IDM: monitor from 2h life to 12hrs. SGA + premies until 36hrs. monitor PG q3-4h before feeds, then before every 2nd or 3rd feed after 48h PG < 1.8 at 2h of life despite one feed or <2.0 after any feed: IV dextrose 2.0-2.6 (or 1.8-2 in first 2h): feed. If repeatedly <2.6, IV dextrose <2.6 and unwell: IV dextrose
33
IV fluid choice for neonatal hypoglycemia
start with D10, can go up to D12
34
developmental dysplasia of the hip risk factors
breech, family hx, female
35
hip dysplasia mangement
positive exam <2wks - ortho referral equivocal exam 2wks+: US or ortho referral tx = pavlik harness (abduction brace)
36
Apgar score
2 for each category: ``` appearance / color pulse (absent, <100, >100) grimace (floppy, weak, vigorous) activity (active, flexed, absent) resp (absent, slow, vigorous) ```